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Time-dependent Improvement of Functional Outcome Following LCS Rotating Platform TKR

M

Martina Hansen's Hospital

Status

Unknown

Conditions

Osteoarthritis
Total Knee Replacement

Treatments

Device: Total Knee Replacement (LCS rotating platform)

Study type

Observational

Funder types

Other

Identifiers

NCT01030848
TKN-001
19039 (NSD) (Registry Identifier)

Details and patient eligibility

About

The objective of this prospective study is to determine (1) the time course of patient-relevant functional outcome evaluated by the Knee injury and Osteoarthritis Outcome Score (KOOS) and (2) the time course of range of motion (ROM) the first four years following TKR using the LCS rotating platform prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest.

Enrollment

50 patients

Sex

All

Ages

40 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with knee osteoarthritis
  • admitted for total knee replacement
  • no rheumatoid arthritis
  • no previous knee infection
  • age 40-85 years

Exclusion criteria

Trial design

50 participants in 1 patient group

Patients with knee osteoarthritis
Treatment:
Device: Total Knee Replacement (LCS rotating platform)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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